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	<title>Comments on: Current TV Presents &#8216;Dying Young&#8217;</title>
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	<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young</link>
	<description>THE FACTS ABOUT CYSTIC FIBROSIS</description>
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		<title>By: TheSecretangel101</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1126</link>
		<dc:creator>TheSecretangel101</dc:creator>
		<pubDate>Sat, 11 Sep 2010 15:05:15 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1126</guid>
		<description>@lilro89  my friends hav cf, it scares me sometimes, but down deep inside i know all of you with cf can do it, just keep on fighting, one day there will be a cure, and jamie your 18 young and strong, you can do it, god is on your side, and we all have faith in you and everyone fighting out there,  good luck jamie, god bless you your a great girl.</description>
		<content:encoded><![CDATA[<p>@lilro89  my friends hav cf, it scares me sometimes, but down deep inside i know all of you with cf can do it, just keep on fighting, one day there will be a cure, and jamie your 18 young and strong, you can do it, god is on your side, and we all have faith in you and everyone fighting out there,  good luck jamie, god bless you your a great girl.</p>
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		<title>By: Ellyb1bubby</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1125</link>
		<dc:creator>Ellyb1bubby</dc:creator>
		<pubDate>Fri, 10 Sep 2010 10:30:28 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1125</guid>
		<description>My bestfriends Sister, Sheana Danielle Blanchard just passed away from CF on March 28th, 2010. She had just turned 21. I wish she didnt have to go, but In a way i&#039;m so happy she left us. She was suffering sooo badly. She couldnt go with out oxygen tanks. RIP Babygirl.</description>
		<content:encoded><![CDATA[<p>My bestfriends Sister, Sheana Danielle Blanchard just passed away from CF on March 28th, 2010. She had just turned 21. I wish she didnt have to go, but In a way i&#8217;m so happy she left us. She was suffering sooo badly. She couldnt go with out oxygen tanks. RIP Babygirl.</p>
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		<title>By: dasjuden27</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1124</link>
		<dc:creator>dasjuden27</dc:creator>
		<pubDate>Wed, 08 Sep 2010 08:38:57 +0000</pubDate>
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		<description>my girlfriend has CF and it kill sme to think that i might not be able to spend my life with her like we talked about.</description>
		<content:encoded><![CDATA[<p>my girlfriend has CF and it kill sme to think that i might not be able to spend my life with her like we talked about.</p>
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		<title>By: kryan364</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1123</link>
		<dc:creator>kryan364</dc:creator>
		<pubDate>Sun, 05 Sep 2010 14:09:04 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1123</guid>
		<description>@TheSecretangel101 
Thank you, she was very strong willed. Siobhan considered the live lung transplant, I have the same blood type she did, but she decided against it..I think it was too risky and her friend did it and then died just two weeks later.</description>
		<content:encoded><![CDATA[<p>@TheSecretangel101<br />
Thank you, she was very strong willed. Siobhan considered the live lung transplant, I have the same blood type she did, but she decided against it..I think it was too risky and her friend did it and then died just two weeks later.</p>
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		<title>By: PrincessMarlena4</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1122</link>
		<dc:creator>PrincessMarlena4</dc:creator>
		<pubDate>Fri, 03 Sep 2010 18:52:11 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1122</guid>
		<description>im so sorry and sad to hear that this is happening with so many people. There so young. i&#039;m so sorry for the suffering you go through. Love you. stay strong. God Bless</description>
		<content:encoded><![CDATA[<p>im so sorry and sad to hear that this is happening with so many people. There so young. i&#8217;m so sorry for the suffering you go through. Love you. stay strong. God Bless</p>
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		<title>By: Tsuki23189</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1121</link>
		<dc:creator>Tsuki23189</dc:creator>
		<pubDate>Tue, 31 Aug 2010 13:36:43 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1121</guid>
		<description>I found this so moving. Im 21 and have CF and I always worry want the future holds for me but we need to face each day with a smile on our faces.</description>
		<content:encoded><![CDATA[<p>I found this so moving. Im 21 and have CF and I always worry want the future holds for me but we need to face each day with a smile on our faces.</p>
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		<title>By: alanmooney147</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1120</link>
		<dc:creator>alanmooney147</dc:creator>
		<pubDate>Mon, 30 Aug 2010 09:46:53 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1120</guid>
		<description>im 29 and have been diagnosed with CF from the age of 1. the one thing i can say to people here is dont let CF get u dwn, its something we must control and put up with but never let it dictate life!! those days when the lungs feel free, live life to the full, enjoy it! one thing ive noticed bout CF sufferers is that we all have the same smile on our faces, never let anything get us down! Im running a marathon in dublin in oct, if i can do it so can u!! Keep fighting and never give up!!!!</description>
		<content:encoded><![CDATA[<p>im 29 and have been diagnosed with CF from the age of 1. the one thing i can say to people here is dont let CF get u dwn, its something we must control and put up with but never let it dictate life!! those days when the lungs feel free, live life to the full, enjoy it! one thing ive noticed bout CF sufferers is that we all have the same smile on our faces, never let anything get us down! Im running a marathon in dublin in oct, if i can do it so can u!! Keep fighting and never give up!!!!</p>
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		<title>By: sheila2022</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1119</link>
		<dc:creator>sheila2022</dc:creator>
		<pubDate>Fri, 27 Aug 2010 11:11:25 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1119</guid>
		<description>This video really moved me it upsets me alos. I have CF im 42 this year. transplant is getting nearer to me now. FEV1 0.66.. stay strong people. xx</description>
		<content:encoded><![CDATA[<p>This video really moved me it upsets me alos. I have CF im 42 this year. transplant is getting nearer to me now. FEV1 0.66.. stay strong people. xx</p>
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		<title>By: internetaddict</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1118</link>
		<dc:creator>internetaddict</dc:creator>
		<pubDate>Wed, 25 Aug 2010 05:34:02 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1118</guid>
		<description>I&#039;m 23 and have cystic fibrosis, and I&#039;m having a lot of trouble with my finances.  I don&#039;t qualify for disability yet, but I am unable to work full time.   I&#039;m going to be aged out of my parent&#039;s health insurance policy soon, and don&#039;t know what to do about health insurance.  What is everyone here doing about their health insurance?  

Thank you very much, keep standing strong and God bless.   .</description>
		<content:encoded><![CDATA[<p>I&#8217;m 23 and have cystic fibrosis, and I&#8217;m having a lot of trouble with my finances.  I don&#8217;t qualify for disability yet, but I am unable to work full time.   I&#8217;m going to be aged out of my parent&#8217;s health insurance policy soon, and don&#8217;t know what to do about health insurance.  What is everyone here doing about their health insurance?  </p>
<p>Thank you very much, keep standing strong and God bless.   .</p>
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		<title>By: talorswift303</title>
		<link>http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young/comment-page-1#comment-1117</link>
		<dc:creator>talorswift303</dc:creator>
		<pubDate>Sun, 22 Aug 2010 20:25:30 +0000</pubDate>
		<guid isPermaLink="false">http://whatiscysticfibrosis.org/cystic-fibrosis/current-tv-presents-dying-young#comment-1117</guid>
		<description>i am also living with cystic fiberosis. i am only 12 years old, and my brother who is 15, also has it. but i was never told i could die from it :(</description>
		<content:encoded><![CDATA[<p>i am also living with cystic fiberosis. i am only 12 years old, and my brother who is 15, also has it. but i was never told i could die from it <img src='http://whatiscysticfibrosis.org/wp-includes/images/smilies/icon_sad.gif' alt=':(' class='wp-smiley' /> </p>
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